Characterization of C-NO Bonds in Nitroaromatic Compounds ...electron correlation effects...
Transcript of Characterization of C-NO Bonds in Nitroaromatic Compounds ...electron correlation effects...
131Characterization of C-NO2 Bonds in Nitroaromatic Compounds:...
Central European Journal of Energetic Materials, 2010, 7(2), 131-144ISSN 1733-7178
Characterization of C-NO2 Bonds in Nitroaromatic Compounds: A Bond Disproportionation Approach
Michal PEXA and Zdeněk FRIEDL
Faculty of Chemistry, Brno University of TechnologyPurkyňova 118, 612 00 Brno, Czech RepublicE-mail: [email protected], [email protected]
Abstract: Homolytic dissociation of C-NO2 bond represents the primary fission process of nitroaromatic compounds under thermal, impact, shock and electric spark initiation stimuli. Homolytic bond dissociation energies BDE(C-NO2) describe the C-NO2 bond fission. Theoretical calculations of BDEs are substantially influenced by inadequate treatment of electron correlation. Recently the alternative method was suggested to overcome this substantial drawback – an isodesmic reaction RC-NO2 + SC-H → RC-H + SC-NO2 where SC-NO2 is standard nitroaromatic compound. This reaction is characterized by bond disproportionation energy DISP(C-NO2), which inherently cancels the electron correlation effect accompanying homolytic bond dissociation energies. The bond disproportionation energies DISP(C-NO2) and bond dissociation energies BDE(C-NO2) were evaluated for 11 nitro benzenes and 19 nitro toluenes at DFT B3LYP/6-311+G(d,p) level and correlated with their detonation velocities, D, and with charge of the most reactive nitro group, Q(NO2).
Keywords: bond dissociation energy, bond disproportionation energy, nitro benzenes, nitro toluenes, detonation velocity
Introduction
Recently computational chemistry is widely used in energetic materials evaluation [1-3]. There are many methods to predict various explosive properties, e.g. heat of explosion, heat of detonation, detonation velocity or sensitivity [4-8]. The study of primary cause of initiation reactivity is in the centre of attention [9, 10]. The idea of fundamental role of nitro group in fission mechanism is
132 M. Pexa, Z. Friedl
greatly accepted. Polynitro compounds are generally known as high energetic materials [11]. The R-NO2 (R can be oxygen, nitrogen, carbon) bond included there is, excluding few cases, the most unstable bond in molecule of polynitro compound. Consequently, the homolytic dissociation of R-NO2 bond represents the primary fission process of nitroaromatic compounds under thermal, impact, shock and electric spark initiation stimuli.
In case of polynitro compounds as nitroaromatics, nitramines and nitramides the C-NO2 or N-NO2 bond fission is mostly characterized by homolytic bond dissociation energies BDE(C-NO2) [10, 12, 13]. Theoretical calculations of homolytic BDEs are substantially influenced by inadequate treatment of electron correlation. This substantial drawback was overcome in previous studies by the isodesmic reaction approach [14, 15]. Isodesmic reactions which are generally used in different type of studies (bond separation reactions, energies of proton-transfer reactions, absolute and relative acidities, etc.) inherently cancel the electron correlation effects accompanying homolytic bond dissociation. The using of closed shells reactants guarantee, that the electron correlation in DISP energy is unimportant. In view of the difference in cost between theoretical calculations of open shell or neutral molecules, the latter seems the perspicuous choice for this purpose.
The concept of isodesmic reaction, which describes C-NO2 bond fission leads to disproportionation energy DISP(C-NO2) by the following series of reactions:
RC-NO2 → RC· + NO2· BDE(RC-NO2) (1)RC-H → RC· + H· BDE(RC-H) (2)
Eq. (1) and Eq. (2) represent the homolytic bond dissociation reaction BDE of specific nitroaromatic and related aromatic compound.
RC-NO2 + H· → RC-H + NO2· BSE(RC-NO2) (3)SC-NO2 + H· → SC-H + NO2· BSE(SC-NO2) (4)
The difference between Eq. (1) and Eq. (2) gives an isodesmic reaction described by Eq. (3) which can be denoted as homolytic bond separation energy BSE(C-NO2). The same sequence of dissociation reaction for standard nitroaromatic molecule SC-NO2 and related aren SC-H leads to homolytic bond separation energy BSE(SC-NO2), Eq. 4.
RC-NO2 + SC-H → SC-NO2 + RC-H DISP(C-NO2) (5)
133Characterization of C-NO2 Bonds in Nitroaromatic Compounds:...
Finally the difference between homolytic bond separation energies BSE(RC-NO2) and BSE(SC-NO2) represents the isodesmic reaction which has already been denoted as bond disproportionation energy DISP(C-NO2) described by Eq. (5) [14,15]. In this paper 30 nitroaromatic compounds were studied by quantum chemical DFT method B3LYP/6-311+G(d,p) and B3LYP/6-31G(d,p) respectively. The evaluated BDE(C-NO2) and DISP(C-NO2) energies were correlated with detonation velocities and charge of the most reactive nitro group.
Calculations
MethodsAll calculations were performed by software Titan [16]. The structures of
nitroaromatics were optimized by DFT B3LYP/6-311+G(d,p) method and the charges of nitro groups were obtained by DFT B3LYP/6-31G(d,p) method. According to the equations mentioned above and from total energies of molecules the values of BDE(C-NO2) and DISP(C-NO2) were obtained and are shown in Table 1. Chemical structures of all studied compounds are summarized in Figure 1 and 2. The bold emphasized nitro groups are the most reactive and so the fission of this bond is the first step of nitroaromatic compounds decomposition. The reactivity of this nitro group was determined according to the nitro group charge method (NGCM) developed by Zhang [17]. The nitro group charges Q(NO2) were computed as a summe of respective atomic charges Q(NO2) = QN + QO1 + QO2
derived by Mulliken population analysis and are summarized in Table 1.
Detonations parametersThe value of detonation velocity, D, was obtained by empirical Rothstein
& Petersen equation [18]. It was chosen because of its good agreement with experimental results and because of its simplicity. The only one disadvantage of this method is the same value of detonation velocity for different isomers. The values of calculated detonation velocities are given in Table 1.
134 M. Pexa, Z. Friedl
Table 1. Total electron energies E, calculated BDE(NO2) energies, DISP(NO2) energies, nitro group charge Q(NO2) and detonation velocities D
Nitroaromatic code
E[a.u.]
BDE[kJ.mol-1]
DISP[kJ.mol-1]
Q(NO2)[e]
D[mm2.μs-2]
1,2-DNB -641.41476 278.17 -57.97 -0.3262 5.841,3-DNB -641.43039 286.66 -16.95 -0.3603 5.841,4-DNB -641.43067 286.95 -16.20 -0.3484 5.841,3,5-TNB -845.98191 276.68 -31.23 -0.3335 7.281,2,4-TNB -845.96766 246.65 -69.38 -0.3091 7.281,2,3-TNB -845.95611 225.24 -98.97 -0.2378 7.281,2,4,5-TeNB -1050.50125 242.46 -78.32 -0.2913 8.131,2,3,5-TeNB -1050.50425 227.85 -107.84 -0.2166 8.131,2,3,4-TeNB -1050.49199 225.17 -102.63 -0.2492 8.13PNB -1255.02233 213.90 -111.16 -0.2336 8.70HNB -1459.55121 225.25 -90.67 -0.2405 9.10o-NT -476.19729 288.24 -10.03 -0.3877 1.63m-NT -476.20172 299.89 1.60 -0.3923 1.63p-NT -476.20271 304.57 4.20 -0.3956 1.632,4-DNT -680.75588 299.66 -26.89 -0.3703 5.102,6-DNT -680.74875 269.72 -31.39 -0.3731 5.103,5-DNT -680.75918 287.46 -15.65 -0.3651 5.102,5-DNT -680.75513 276.18 -26.26 -0.3597 5.103,4-DNT -680.74448 254.32 -56.84 -0.3305 5.102,3-DNT -680.74339 251.42 -57.09 -0.3042 5.102,4,6-TNT -885.30018 255.22 -50.20 -0.3512 6.672,3,5-TNT -885.29622 242.44 -69.24 -0.2813 6.672,3,4-TNT -885.28481 233.12 -90.54 -0.2630 6.672,4,5-TNT -885.29323 246.91 -68.44 -0.3039 6.673,4,5-TNT -885.28670 235.53 -94.24 -0.2453 6.672,3,6-TNT -885.29085 237.73 -72.73 -0.2965 6.672,3,5,6-TeNT -1089.82880 234.58 -80.96 -0.2751 7.602,3,4,6-TeNT -1089.82718 226.29 -95.60 -0.2439 7.602,3,4,5-TeNT -1089.82300 236.21 -96.30 -0.2543 7.60PNT -1294.35404 225.17 -100.25 -0.2592 8.24
135Characterization of C-NO2 Bonds in Nitroaromatic Compounds:...
NO2 NO2
NO2
NO2
NO2
NO2
NO2
NO2
NO2
NO2
NO2
NO2
NO2
NO2
NO2O2N
NO2
NO2
NO2
O2N
NO2
NO2
NO2
NO2
NO2
NO2O2N
NO2
NO2
NO2O2N
O2N NO2
NO2
NO2O2N
O2N NO2
NO2
nitrobenzene 1,2-dinitrobenzene 1,3-dinitrobenzene 1,4-dinitrobenzene 1,2,3-trinitrobenzene 1,2,4-trinitrobenzene 1,3,5-trinitrobenzene
1,2,4,5-tetranitrobenzene 1,2,3,5-tetranitrobenzene 1,2,3,4,5-pentanitrobenzene hexanitrobenzene
NB 1,2-DNB 1,3-DNB 1,4-DNB 1,2,3-TNB 1,2,4-TNB 1,3,5-TNB
1,2,3,4-TeNB 1,2,4,5-TeNB 1,2,3,5-TeNB PNB HNB
Figure 1. The chemical structures of nitro benzenes with bold emphasized the most reactive nitro group.
CH3
NO2
CH3
NO2
CH3
NO2
CH3
NO2
NO2
CH3
NO2
NO2
CH3
NO2
O2N
CH3
NO2O2N
CH3
NO2
NO2
CH3
NO2O2N
CH3
NO2
NO2
NO2
CH3
NO2
NO2O2N
CH3
NO2
NO2
O2N
CH3
NO2O2N
NO2
CH3
NO2
NO2
O2N
CH3
NO2
NO2
O2N
CH3
NO2
NO2
NO2
O2N
CH3
NO2
NO2
O2N
O2N
CH3
NO2
NO2
O2N
NO2
CH3
NO2
NO2
O2N
NO2
O2N
2-nitrotoluene 3-nitrotoluene 4-nitrotoluene 2,3-dinitrotoluene 2,4-dinitrotoluene2-NT 3-NT 4-NT 2,3-DNT 2,4-DNT 2,5-DNT
2,5-dinitrotoluene
2,6-dinitrotoluene
3,4-dinitrotoluene
3,5-dinitrotoluene 2,3,4-trinitrotoluene 2,3,5-trinitrotoluene 2,3,6-trinitrotoluene
2,4,6-trinitrotoluene
2,6-DNT
3,4-DNT
3,5-DNT 2,3,4-TNT 2,3,5-TNT 2,3,6-TNT
2,4,6-TNT
2,4,5-trinitrotoluene 3,4,5-trinitrotoluene 2,3,4,5-tetranitrotoluene 2,3,5,6-tetranitrotoluene
2,3,4,6-tetranitrotoluene pentanitrotoluene
2,4,5-TNT 3,4,5-TNT 2,3,4,5-TeNT 2,3,5,6-TeNT
2,3,4,6-TeNT PNT
Figure 2. The chemical structures of nitro toluenes with bold emphasized the most reactive nitro group.
136 M. Pexa, Z. Friedl
Results and discussion
In few recently published papers [19, 20] was proofed that exists logical relationship between low-temperature thermal decomposition characteristics and initiation of detonation. The Evans-Polanyi-Semanov (E-P-S) equation (6) was formulated in Ref. [21]. In this relationship the homolytic character of primary fission was the motive factor to study micro-mechanism of energetic materials initiations.
E = αQdet + β (6)
Application of relationship Eq. (7), between Heat of explosion Qdet and detonation velocity D:
2
det 22(γ – 1)DQ = (7)
where γ is the polytropy coefficient, leads to Eq. (8). This equation was called modified E-P-S [21].
E = aD2 + b (8)
The original E-P-S describes a relationship between activation energy of free radical substitution reactions and corresponding heats of reactions DH. Eq. (8) indicates that strength of the bond being split is critical factor in given reaction.
The energy, E, in both equations (6) and (8) can be the activation energy of thermal decomposition, Ea, or any other energy value which characterizes the reaction, e.g. the energy of electric spark − EES, drop energy – Ep or charge of the most reactive nitro group in given molecule. If the energy, E, in Eq. (8) is substituted by BDE energy of nitro benzenes the relationship is displayed on Figure 3. Analogically for nitro toluenes, the dependence of BDE to square of detonation velocity, D2, is on Figure 4. Similarly, the energy E in Eqs. (6) and (8) can be substituted by bond dispro portionation energy, DISP(C-NO2). Than the Figures 3 and 4 transform to Figures 5 and 6.
137Characterization of C-NO2 Bonds in Nitroaromatic Compounds:...
Figure 3. Dependence of BDE of nitro benzenes to square of detonation velocity.
Figure 4. Dependence of BDE of nitro toluenes to square of detonation velocity.
There are few different lines in both kinds of dependences, DISP and BDE to D2. They are strictly influenced by structure of given molecules. In case of nitro benzenes, the first line (the continuous one) contains just co-planar structures (1,3-DNB; 1,4-DNB and 1,3,5-TNB). This series is primarily influenced by structural fragment CHC(NO2)CH.
138 M. Pexa, Z. Friedl
NO2
NO2
NO2
NO2
NO2
NO2O2N
Figure 5. Nitro benzenes containing CHC(NO2)CH structural fragment.
The second line (dashed one) contains molecules, which has in structure 2 nitro groups in neighborhood (1,2-DNB; 1,2,4-TNB; 1,2,4,5-TeNB and HNB). The important part of structure is fragment C(NO2)C(NO2) .
NO2
NO2
NO2
NO2
NO2
NO2
NO2
NO2
O2N
NO2
NO2O2N
O2N NO2
NO2
Figure 6. Nitro benzenes containing C(NO2)C(NO2) structural fragment.
Finally, the third line (dotted one) contains three consecutive nitro groups (1,2,3-TNB; 1,2,3,5-TeNB; 1,2,3,4-TeNB and PNB).
NO2
NO2
NO2
NO2
NO2
NO2
NO2
NO2
NO2O2N
NO2
NO2
NO2O2N
O2N NO2
Figure 7. Nitro benzenes containing C(NO2)C(NO2)C(NO2) structural fragment.
Analogously for nitro toluenes, there are again few different lines which describe different structure. There are co-planar structures (m-NT; p-NT; 3,5-DNT),
CH3
NO2
CH3
NO2
CH3
NO2O2N
Figure 8. Nitro toluenes containing CHC(NO2)CH structural fragment.
139Characterization of C-NO2 Bonds in Nitroaromatic Compounds:...
further molecules with two adjacent nitro groups anywhere on aromatic ring (2,3-DNT; 3,4-DNT; 2,4,5-TNT; 2,3,5-TNT; 2,3,6-TNT; 2,3,5,6-TeNT)
CH3
NO2
NO2
CH3
NO2
NO2
O2N
CH3
NO2
NO2O2N
CH3
NO2
NO2
O2N
CH3
NO2
NO2
O2N
O2N
CH3
NO2
NO2
Figure 9. Nitro toluenes containing C(NO2)C(NO2) structural fragment.
and molecules with three consecutive nitro groups (2,3,4-TNT; 3,4,5-TNT; 2,3,4,5-TeNT; 2,3,4,6-TeNT; PNT).
CH3
NO2
NO2
NO2
CH3
NO2
NO2
O2N
CH3
NO2
NO2
NO2
O2N
CH3
NO2
NO2
O2N
NO2
CH3
NO2
NO2
O2N
NO2
O2N
Figure 10. Nitro toluenes containing C(NO2)C(NO2)C(NO2) structural fragment.
Moreover, in structure of nitro toluenes is a methyl group which determines new group (dash-and-dotted one). This group has NO2 next to methyl and from the other side of NO2 is hydrogen bonded (o-NT; 2,6-DNT; 2,5-DNT; 2,4-DNT; 2,4,6-TNT).
CH3
NO2
NO2
CH3
NO2
O2N
CH3
NO2O2N
CH3
NO2O2N
NO2
Figure 11. Nitro toluenes containing C(CH3)C(NO2)CH structural fragment.
It has to be explained why 2,4-DNT and 2,4,6-TNT are excluded from plots in Figure 4. Both of them have in structure C(CH3)C(NO2)CH, but they differ by the pathway of decomposition. Many papers were written to describe the decomposition of nitro aromatics [22-24]. From these studies is known that 2,4-DNT has a special way of decomposition [22]. That is why the 2,4-DNT is out of corresponding curve. Instead of C-NO2 fission, the splitting of N-OH bond in aci-form is the first step of disintegration (see Figure 12). 2,4,6-TNT should behave similarly, but Cohen et al. [25] find latter pathway which afterwards leads
140 M. Pexa, Z. Friedl
to water elimination and formation of dinitroanthranil.
C
NO2
N+
O-
O
HH H C
NO2
N+
O
O-
HH H
Figure 12. Mechanism of 2,4-DNT rearrangement.
On the next two Figures 13 and 14 are shown dependences of DISP energy to square of detonation velocity. In comparison to dependences of BDE energy to D2 the higher regression coefficients are seen. Much better distinguishing of structure also results from this comparison. In case of nitro toluenes, interesting thing is that above mentioned exceptions 2,4-DNT and 2,4,6-TNT fit the corresponding curve significantly closely. It seems to be probable that DISP energy is independent of the way of decomposition.
Figure 13. Dependence of DISP of nitro benzenes to square of detonation velocity.
141Characterization of C-NO2 Bonds in Nitroaromatic Compounds:...
Figure 14. Dependence of DISP of nitro toluenes to square of detonation velocity.
The substitution of the energy E in Eq. (8) by the DISP energy and simultaneously the square of detonation velocity D2 by nitro group charge Q(NO2) leads to the relationship between DISP energies and charges Q(NO2) and shown for series of nitro benzenes in Figure 15 and for nitro toluenes in Figure 16, respectively. Both plots are characterized by single regression lines with high correlation coefficients (r = 0.93 and 0.95) which describe the expected indirect rule of proportion between ease of bond fission (decrease of DISP value) and nitro group charge (increase of positive charge). Nevertheless, the structural selectivity of DISP vs. D2 relationships was lost. But changes in charges are too small (ΔQ(NO2) ~ 0.14 e) in comparison with changes of energy (ΔE ~ 100 kJ.mol-1) and it could be note that both quantities are structure oriented parameters with high covariance and their use should be done separately. Recently, the alternative approach based on electrostatic potentials was developed [26, 27] and a comparison with results obtained would be needed in future.
142 M. Pexa, Z. Friedl
1,4-DNB
1,3-DNB
1,3,5-TNB
1,2,4,5-TeNBHNB
1,2,3,4-TeNBPNB
1,2,3,5-TeNB
1,2,4-TNB
-1,2-DNB
1,2,3-TNB
y = -669,39x - 261,75R2 = 0,9308
-130
-110
-90
-70
-50
-30
-10
10
-0.38 -0.33 -0.28 -0.23
Q [e]
DIS
P [k
J.m
ol-1
]
Figure 15. Dependence of DISP of nitro benzenes to the charges of the most reactive nitro group.
o-NT
2,3,4,6-TeNT
p-NT
2,6-DNT
2,4-DNT
2,4,6-TNT
2,3,5,6-TeNT
PNT
m-NT
3,5-DNT2,5-DNT
3,4-DNT
2,3-DNT
2,4,5-TNT2,3,6-TNT
2,3,5-TNT
2,3,4-TNT
2,3,4,5-TeNT
3,4,5-TNT
y = -630,07x - 255,26R2 = 0,9494
-120
-100
-80
-60
-40
-20
0
20
-0.40 -0.35 -0.30 -0.25 -0.20Q [e]
DIS
P [k
J.m
ol-1
]
Figure 16. Dependence of DISP of nitro toluenes on the charges of the most reactive nitro group.
Conclusion
In this study the disproportionation energies of an isodesmic reaction RC-NO2 + SC-H → SC-NO2 + RC-H proved to be an alternative measure of initiation mechanisms of nitro aromatic energetic materials. Comparison of relationships
143Characterization of C-NO2 Bonds in Nitroaromatic Compounds:...
between DISP energies and square of detonation velocity D2 for series of nitro benzenes and toluenes reveals the higher selectivity to molecular structure for DISP than BDE energies. The property of DISP energies to describe structure-property relationships is similar to findings also in other CHNO energetic materials as nitramines and nitramides. Regarding the detonation as a “zero-order reaction” the findings given above lead to the construction of SPRS model where DISP energies could be considered as structural Hammett-like constants.
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